FDA Medical Device Recalls (openFDA)
Zimmer Inc.: Zimmer Hemovac Wound Drainage Device Infection Control Kits, Catalog Number/ REF 00-2550-050-10; 400 ml Infection Control Comp. Kit, sterile, latex free, Rx only; Sold in packages of 10, which contain packages of 1 and 5; Zimmer U.K. Ltd., Swindon, Wiltshire, United Kingdom; Zimmer, Dover, Ohio.
- Recall number
- Z-1452-2008
- Recalling firm
- Zimmer Inc.
- Product
- Zimmer Hemovac Wound Drainage Device Infection Control Kits, Catalog Number/ REF 00-2550-050-10; 400 ml Infection Control Comp. Kit, sterile, latex free, Rx only; Sold in packages of 10, which contain packages of 1 and 5; Zimmer U.K. Ltd., Swindon, Wiltshire, United Kingdom; Zimmer, Dover, Ohio.
- Status
- Terminated
- Initiated
- 2008-01-31
- Posted
- 2008-04-09
- Terminated
- 2009-11-12
- Reason
- Leakage; The kits may disassemble at the fluid collection port, which would present a risk of exposure to blood borne pathogens to health care providers should it occur during use.
- Root cause
- Process control
- Action
- Consignees were notified via Urgent Infection Control Recall letter dated 1/31/08 to examine their inventory and return the recalled lots. Custom kit packers were instructed in the same letter to recall these products/lots from their own customers.
- Quantity
- 34,354 (Recalls Z-1448/1458-2008)
- Distribution
- Worldwide-USA, Australia, Canada, Colombia, Denmark, Dubai, Italy, Japan, Mexico and Singapore.
- Lot, serial or model codes
- Lot Numbers: 60006819, 60015774, 60033386, 60045263, 60057329, 60067689, 60084095, 60094656, 60106763, 60116383, 60126841, 60145039, 60158789, 60171589, 60184524, 60200855, 60215687, 60230182, 60240753, 60262574, 60278454, 60294877, 60321541, 60333502, 60342988, 60354480, 60371375, 60385890, 60402653, 60412505, 60437090, 60471395, 60506574, 60520507, 60551036, 60570976, 60590576, 60612123 and 60626622.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- GCY
- Firm FEI
- 1000220733
- Firm city
- Warsaw
- Firm state
- IN
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28